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High-throughput testing in head and neck squamous cell carcinoma identifies agents with preferential activity in human papillomavirus-positive or negative cell lines.

Authors :
Ghasemi F
Black M
Sun RX
Vizeacoumar F
Pinto N
Ruicci KM
Yoo J
Fung K
MacNeil D
Palma DA
Winquist E
Mymryk JS
Ailles LA
Datti A
Barrett JW
Boutros PC
Nichols AC
Source :
Oncotarget [Oncotarget] 2018 May 25; Vol. 9 (40), pp. 26064-26071. Date of Electronic Publication: 2018 May 25 (Print Publication: 2018).
Publication Year :
2018

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a common cancer diagnosis worldwide. Despite advances in treatment, HNSCC has very poor survival outcomes, emphasizing an ongoing need for development of improved therapeutic options. The distinct tumor characteristics of human papillomavirus (HPV)-positive vs . HPV-negative disease necessitate development of treatment strategies tailored to tumor HPV-status. High-throughput robotic screening of 1,433 biologically and pharmacologically relevant compounds at a single dose (4 μM) was carried out against 6 HPV-positive and 20 HPV-negative HNSCC cell lines for preliminary identification of therapeutically relevant compounds. Statistical analysis was further carried out to differentiate compounds with preferential activity against cell lines stratified by the HPV-status. These analyses yielded 57 compounds with higher activity in HPV-negative cell lines, and 34 with higher-activity in HPV-positive ones. Multi-point dose-response curves were generated for six of these compounds (Ryuvidine, MK-1775, SNS-032, Flavopiridol, AZD-7762 and ARP-101), confirming Ryuvidine to have preferential potency against HPV-negative cell lines, and MK-1775 to have preferential potency against HPV-positive cell lines. These data comprise a valuable resource for further investigation of compounds with therapeutic potential in the HNSCC.<br />Competing Interests: CONFLICTS OF INTEREST The authors declare no potential conflicts of interest.

Details

Language :
English
ISSN :
1949-2553
Volume :
9
Issue :
40
Database :
MEDLINE
Journal :
Oncotarget
Publication Type :
Academic Journal
Accession number :
29899842
Full Text :
https://doi.org/10.18632/oncotarget.25436